Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
CWF19L1 Gene Spinocerebellar ataxia type 17, autosomal recessive NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
IFRD1 Gene Spinocerebellar ataxia type 18, autosomal dominant NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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AIFM1 Gene Combined oxidative phosphorylation deficiency type 6 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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AIFM1 Gene Deafness, X-linked type 5 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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AIFM1 Gene CMTX4 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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Mayo Clinic Laboratories Mayo Clinic United States | 1 | 211 |
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Peripheral Neuropathy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 186 |
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Comprehensive Epilepsy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 318 |
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Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
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Motor and Sensory Neuropathy Panel Mayo Clinic Laboratories Mayo Clinic United States | 2 | 87 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 25 | 25 |
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Molecular Genetics Laboratory London Health Sciences Centre Canada | 46 | 34 |
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Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
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Genomic Unity® Nuclear Encoded Mitochondrial Gene Analysis Variantyx, Inc. United States | 1 | 335 |
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AudioloGene Hearing Loss Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 200 |
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Nuclear Mitochondrial Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 221 |
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Combined mtDNA+Nuclear Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 12 | 221 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
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AIFM1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.